岩石2
岩石1
Rho相关蛋白激酶
神经退行性变
罗亚
中枢神经系统
肌萎缩侧索硬化
再生(生物学)
神经科学
生物
蛋白激酶B
法苏迪尔
细胞生物学
激酶
基因亚型
信号转导
医学
神经突
疾病
病理
基因
体外
生物化学
作者
Cheong‐Meng Chong,Nana Ai,Simon Ming‐Yuen Lee
标识
DOI:10.2174/1389450117666160401123825
摘要
Rho-associated protein kinase (ROCK) is a serine-threonine kinase originally identified as a crucial regulator of actin cytoskeleton. Recent studies have defined new functions of ROCK as a critical component of diverse signaling pathways in neurons. In addition, inhibition of ROCK causes several biological events such as increase of neurite outgrowth, axonal regeneration, and activation of prosurvival Akt. Thus, it has attracted scientist's strong attentions and considered ROCK as a promising therapeutic target for the treatment of neurodegenerative disorders including Alzheimer disease, Parkinson's disease, Huntington';s disease, multiple sclerosis, and amyotrophic lateral sclerosis. However, ROCK has two highly homologous isoforms, ROCK1 and ROCK2. Accumulated evidences indicate that ROCK1 and ROCK2 might involve in distinct cellular functions in central nervous system (CNS) and neurodegenerative processes. This review summarizes recent updates regarding ROCK isoformspecific functions in CNS and the progress of ROCK inhibitors in preclinical studies for neurodegenerative diseases.
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